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μ-Oxo-bis[(octacosafluoro-meso-tetraphenylporphyrinato)iron(iii)] – synthesis, crystal structure, and catalytic activity in oxidation reactions

We describe the synthesis and X-ray crystal structure of μ-oxo-bis[(octacosafluoro-meso-tetraphenylporphyrinato)iron(iii)] [(FeTPPF(28))(2)O]. This novel iron complex is an efficient catalyst for oxidative biaryl coupling reactions of diarylamines and carbazoles. The asymmetric oxidative coupling in...

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Detalles Bibliográficos
Autores principales: Schuh, Tristan, Kataeva, Olga, Knölker, Hans-Joachim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9811517/
https://www.ncbi.nlm.nih.gov/pubmed/36687339
http://dx.doi.org/10.1039/d2sc06083c
Descripción
Sumario:We describe the synthesis and X-ray crystal structure of μ-oxo-bis[(octacosafluoro-meso-tetraphenylporphyrinato)iron(iii)] [(FeTPPF(28))(2)O]. This novel iron complex is an efficient catalyst for oxidative biaryl coupling reactions of diarylamines and carbazoles. The asymmetric oxidative coupling in the presence of an axially chiral biaryl phosphoric acid as co-catalyst provides the 2,2′-bis(arylamino)-1,1′-biaryl in 96% ee. The Wacker-type oxidation of alkenes to the corresponding ketones with (FeTPPF(28))(2)O as catalyst in the presence of phenylsilane proceeds at room temperature with air as the terminal oxidant. For internal and aliphatic alkenes increased ketone/alcohol product ratios were obtained.